Ban Liquid
Product Images NDC 10596-337

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ban (NDC 10596-337). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kao Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

10596-337-15-updated (10596 337 15 Updated)

Label images of Ban Roll-On Antiperspirant Deodorant Powder Fresh containing 18% Aluminum Chlorohydrate in a 20 g/103 mL liquid topical dosage form. The front panel shows the product name and that it is fragrance-free. The back panel includes a Drug Facts label detailing active ingredient, purpose, usage instructions, warnings, and other product information as supplied by Kao USA Inc.*

FDA Label Image

Label (10596 337 35 Update)

Packaging label of Ban Roll-On Antiperspirant Deodorant Powder Fresh liquid topical product. The front label shows the brand name Ban with Powder Fresh scent, an invisible roll-on delivery, and a 3.5 FL OZ (103 mL) size. The back label includes Drug Facts with the active ingredient Aluminum Chlorohydrate 17.60% as an antiperspirant, usage instructions, warnings, inactive ingredients, and manufacturer details by Kao USA Inc.*

FDA Label Image

10596-337-70-updated (10596 337 70 Updated)

Ban Roll-On Antiperspirant Deodorant Powder Fresh, liquid topical antiperspirant with 20 g/103 mL strength by Kao USA Inc. The label indicates a value pack with 2 units, featuring warnings, directions, inactive ingredients, and contact information. The packaging highlights the product's antiperspirant purpose and sustainable sourcing certifications.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.